Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912584Generated: November 2, 2026

Sodium Carbonate → 1,4-dimethyl-5-(4-fluorophenyl)-1H-pyrrole-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/912584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Fluorophenylboronic acidHCID 285645—
Reactantethyl 5-bromo-1,4-dimethyl-1H-pyrrole-3-carboxylateHCID 59808055—
CatalystHCID 178418397HCID 178418397—
SolventDichloromethaneHCID 6344—
SolventN,N-Dimethylformamide--water (1/1)HCID 21962138—
Product1,4-dimethyl-5-(4-fluorophenyl)-1H-pyrrole-3-carboxylic acid ethyl esterHCID 6725316296.4%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of ethyl 5-bromo-1,4-dimethyl-1H-pyrrole-3-carboxylate (246 mg, 1.0 mmol), 4-fluorophenyl-boronic acid (210 mg, 1.5 mmol), Na2CO3 (320 mg, 3.0 mmol) and Pd(PPh3)4 (116 mg, 0.10 mmol) in DMF/H2O (10:1, 10 mL) was sparged with nitrogen for 10 min. The reaction vial was sealed and heated at 110° C. with stirring. After 18h, the reaction mixture was diluted with DCM and then filtered. The filtrate was concentrated under reduced pressure and then purified by column chromatography, eluting with EtOAc-Hex (0:100 to 50:50), to give 1,4-dimethyl-5-(4-fluorophenyl)-1H-pyrrole-3-carboxylic acid ethyl ester (252 mg, 96%) as a pale yellow solid. 1H-NMR (CDCl3): δ 7.30 (1H, s), 7.26-7.20 (2H, m), 7.15-7.10 (2H, m), 4.28 (2H, q), 3.48 (3H, s), 2.20 (3H, s), 1.36 (3H, t). MS (ESI): 262 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026237B2
Source datasetuspto-grants-2011_09
ORD IDord-7b657cbe708245d9bb6df9f4b3ddabe9
Source noteuspto-grants-2011_09